A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567876



Internal ID20940947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77744608..77745000hg38UCSC Ensembl
chr7:77373925..77374317hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276642
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567876
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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